# Identification of natural variants that influence responses to ethanol in C. elegans

> **NIH NIH R01** · VIRGINIA COMMONWEALTH UNIVERSITY · 2020 · $336,574

## Abstract

PROJECT SUMMARY
 Genetic variation in humans contributes to an individual's likelihood to develop an alcohol use disorder. The
genetic variation that influences alcohol abuse liability is therefore an important target for study, but it has been
difficult to identify specific liability genes. Laboratory studies in animal models have been extremely useful in
elucidating the molecular pharmacology of alcohol (ethanol), but laboratory derived genetic manipulations
rarely model the naturally occurring genetic variation that is observed in wild populations. As such, predicting
relevant human allelic variation has been difficult. Here, we study the natural allelic variation found in wild
strains of the the nematode worm Caenorhabditis elegans to identify alleles that are tolerated in the wild and
can modulate the function of pathways that impact physiological responses to ethanol. C. elegans is an
important model species with demonstrated relevance to humans; there is striking conservation between the
machinery of nervous system function in worms and humans, and genes that influence ethanol response
behaviors in worms also influence the likelihood to develop alcohol use disorders in humans.
 This collaborative proposal brings together the diverse expertise of two laboratories. We take advantage of a
unique resource, recombinant inbred lines (RILs) derived from four genetically diverse wild strains to identify
natural allelic variation that can modulate the effects of ethanol. We have shown that the parent wild-type
strains and the derived RILs display a range of phenotypes in different behavioral responses ethanol. We will
exploit the efficiency and ease of manipulating the C. elegans model to carry out high throughput analyses that
will identify genetic variation that alters behavioral and/or transcriptional responses to ethanol. We will directly
test the causal nature of candidate ethanol response allelic variants, identified by quantitative trait locus
mapping, through the use of gene editing techniques (CRISPR-Cas9) to introduce the allele into strains that
carry different alleles. The ability to compare and contrast the influence of genetic variants on different
responses to ethanol brings further power to our analyses. We will identify the genes that impact the
physiological responses in each behavior uniquely, and second, we will identify genes that affect the
behavioral responses across ethanol response phenotypes. We will also assess the impact of alleles that
modulate transcription in response to ethanol on behavioral responses. These different analyses can inform us
of the molecular mechanisms underlying these different responses to ethanol.
 Together, these studies will provide both specific and more general novel insights into the neurogenetics of
ethanol. We will establish the degree to which genetic variation in known or novel biological pathways that
mediate or modulate the effect of ethanol can change responses to ethanol and the degree...

## Key facts

- **NIH application ID:** 9976403
- **Project number:** 5R01AA026658-03
- **Recipient organization:** VIRGINIA COMMONWEALTH UNIVERSITY
- **Principal Investigator:** JILL C BETTINGER
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $336,574
- **Award type:** 5
- **Project period:** 2018-08-01 → 2023-07-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/9976403

## Citation

> US National Institutes of Health, RePORTER application 9976403, Identification of natural variants that influence responses to ethanol in C. elegans (5R01AA026658-03). Retrieved via AI Analytics 2026-05-22 from https://api.ai-analytics.org/grant/nih/9976403. Licensed CC0.

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